Patau Syndrome, also known as Trisomy 13, can lead to serious birth defects and severe intellectual disability. Patient with Patau syndrome has life expectancy of less than 1 year.

Down Syndrome, also known as Trisomy 21, can lead to birth defects of the heart or other organs, such as hearing and vision problems.

Monosomy X, also known as Turner Syndrome, is a condition that only affects female. It can cause a variety of medical and developmental problems, including heart defects, learning disabilities and short height.

Klinefelter Syndrome is characterized by the presence of an extra X chromosome in the cells of a male. The primary features are infertility and impaired development of the sexual organs.

1p36 Deletion Syndrome is a congenital genetic disorder that affects intellectual and behavioural developments, as well as heart abnormalities.

2q33.1 deletion syndrome is a rare chromosomal disease with a highly variable phenotype typically characterized by significant feeding difficulties, delayed growth, cleft palate, and behavioural issues.

5p deletion, also known as Cri-du-chat Syndrome, is a chromosomal condition that causes feeding and breathing difficulties, smaller head size, low birth weight, and hypotonia in infancy.

22q11.2 Deletion Syndrome, also known as DiGeorge Syndrome, can affect the heart, immune system, and kidney of the infant. Patient may also suffer from feeding difficulties, epilepsy, and mild to moderate intellectual disability.

8q24.1 Deletion Syndrome, also known as Langer-Giedion Syndrome, is an uncommon genetic disorder with characteristic craniofacial appearance includes a bulbous nose, an elongated upper lip, a long philtrum and sparse hair.

15q11.2 Deletion Syndrome, also known as Prader-Willi Syndrome, is a genetic disorder that can increase the risk of obesity and hypotonia in childhood.